Have questions? Visit https://www.reddit.com/r/SNPedia

rs367797185

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs367797185(C;T)
Make rs367797185(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position63483494
GeneACE
is asnp
is mentioned by
dbSNPrs367797185
ebirs367797185
HLIrs367797185
Exacrs367797185
Varsomers367797185
Maprs367797185
PheGenIrs367797185
hapmaprs367797185
1000 genomesrs367797185
hgdprs367797185
ensemblrs367797185
gopubmedrs367797185
geneviewrs367797185
scholarrs367797185
googlers367797185
pharmgkbrs367797185
gwascentralrs367797185
openSNPrs367797185
23andMers367797185
23andMe allrs367797185
SNP Nexus

SNPshotrs367797185
SNPdbers367797185
MSV3drs367797185
GWAS Ctlgrs367797185
Max Magnitude0
ClinVar
Risk rs367797185(T;T)
Alt rs367797185(T;T)
Reference rs367797185(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ACE
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.61560855C>T
CLNSRC
CLNACC RCV000224863.1,